US4710544A - Thermoplastic composition of polyolefin and high ethylene content ethylene/alkyl acrylate elastomer - Google Patents
Thermoplastic composition of polyolefin and high ethylene content ethylene/alkyl acrylate elastomer Download PDFInfo
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- US4710544A US4710544A US07/017,332 US1733287A US4710544A US 4710544 A US4710544 A US 4710544A US 1733287 A US1733287 A US 1733287A US 4710544 A US4710544 A US 4710544A
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/10—Homopolymers or copolymers of propene
- C08L23/12—Polypropene
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/04—Homopolymers or copolymers of ethene
- C08L23/06—Polyethene
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/04—Homopolymers or copolymers of ethene
- C08L23/08—Copolymers of ethene
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/04—Homopolymers or copolymers of ethene
- C08L23/08—Copolymers of ethene
- C08L23/0846—Copolymers of ethene with unsaturated hydrocarbons containing other atoms than carbon or hydrogen atoms
- C08L23/0869—Acids or derivatives thereof
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2312/00—Crosslinking
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L91/00—Compositions of oils, fats or waxes; Compositions of derivatives thereof
Definitions
- Nonpolar olefin polymers e.g., polypropylene resin
- polar acrylate ester copolymers e.g., ethylene/alkyl acrylate elastomers
- the low degree of compatibility of the polymers with each other is evident from the lack of development in the blends of good physical properties, especially tensile strength and elongation at break and, consequently, such blends cannot be used for many applications such as tubing, seals, hose covers, and wire and cable coverings when high tensile strength and elongation at break are required.
- the compatibilizing agents for polyolefins are copolymers that have at least one olefin polymer compatibilizing segment derived from a homopolymer or copolymer of a C 2 -C 8 alpha-monoolefin or polybutadiene, polyisoprene or a polyalkenamer, and at least one acrylic ester copolymer rubber compatibilizing segment derived from a polymer selected from epichlorohydrin polymers, nitrile rubber, urethane polymers, vinyl chloride polymers, polyamides, polyamines, polyesters, and crosslinkable acrylic ester copolymer rubbers.
- the requirement that the blend of polymers must contain a compatibilizing agent to make a product having excellent physical properties adds to the expense of the polymer blend and requires an extra step for manufacturing the thermoplastic composition
- thermoplastic compositions are especially useful for molding parts such as seals, gaskets, and sheeting for automotive applications, e.g., doors or fenders, and wire and cable covering.
- the present invention is directed to a thermoplastic composition having excellent tensile strength and elongation at break values. More specifically, this invention is directed to a melt processible thermoplastic composition comprising a blend of:
- a crosslinked ethylene/alkyl acrylate elastomer made from dynamically crosslinking an ethylene/alkyl acrylate/monoalkyl ester of 1,4-butenedioic acid copolymer containing about 60-90 weight percent ethylene, preferably 65-80 weight percent, and wherein the alkyl group of the alkyl acrylate contains 1-6 carbon atoms, the dynamically crosslinked elastomer being dispersed throughout the crystalline
- the melt processible multi-phase thermoplastic composition comprising a blend of a crystalline polyolefin resin and a dynamically crosslinked elastomer
- a dynamically crosslinked elastomer can be prepared by mixing and shearing an uncrosslinked elastomeric ethylene, alkyl acrylate copolymer containing a cure site monomer, i.e., the monoalkyl ester of 1,4-butenedioic acid, with a crystalline polyolefin resin and a crosslinking agent for the elastomer, preferably in a high shear mixer, and carrying out crosslinking of the ethylene, alkyl acrylate copolymer having a cure site and containing about 60-90 weight percent ethylene simultaneously with the mixing operation.
- a cure site monomer i.e., the monoalkyl ester of 1,4-butenedioic acid
- the dynamically crosslinked ethylene, alkyl acrylate elastomer component must contain at least 60 weight percent ethylene, otherwise the composition will have inadequate tensile strength and inadequate elongation at break values, which indicate that the polymer components of the composition are not compatible and their use is restricted.
- the melt processible multi-phase thermoplastic compositions can be formed into various shapes by compression molding, injection molding, blow molding and extrusion procedure.
- the compositions can be used for automotive parts, e.g., automotive boots, seals, gaskets, tubing, reinforced hose, film, sheeting, and wire cable coverings and show high tensile strength and elongation at break values in spite of the fact the composition does not contain a compatibilizing agent.
- the crystalline polyolefin resin used in the present invention is polyethylene, polypropylene or copolymers thereof and is added to and is present in the composition in amounts of from about 15-75 parts by weight, preferably, 25-70 parts by weight.
- polyethylene and polypropylene as used herein are intended to include, in addition to the homopolymers, those polymers that also contain minor amounts, usually not greater than 15 weight percent, of higher alpha-olefins, e.g., those containing 3-8 carbon atoms, e.g., butene, octene etc.
- the polyethylene and the polypropylene polymers used in this invention have melt indices in the range of from about 0.07-80 dg/min. Polypropylene is the preferred resin because of the superior properties it imparts to the composition, especially improved heat resistance.
- the melt processible thermoplastic compositions also contain 25-85 parts by weight, preferably 30-75 parts by weight, of a dynamically crosslinked elastomer which comprises ethylene, an alkyl acrylate wherein the alkyl group contains 1-6 carbon atoms.
- the elastomer is made from dynamically crosslinking an ethylene/alkyl acrylate/monoalkyl ester of 1,4-butenedioic acid copolymer, the latter monomer of the elastomer functioning as a cure site.
- the polyolefin and the dynamically crosslinked ethylene/alkyl acrylate elastomer are compatible provided that the amount of ethylene in the elastomeric copolymer is at least about 60 weight percent, preferably at least about 65 weight percent.
- the excellent compatibility of the blends of the thermoplastic compositions, without the necessity of incorporating a compatibilizing agent for the nonpolar polyolefin and the polar elastomeric copolymer, is shown by the high tensile strength values and high elongation at break values obtained.
- the dynamically crosslinked ethylene/alkyl acrylate elastomer component of the blend usually does not contain more than about 90 weight percent of ethylene, preferably not more than about 80 weight percent ethylene.
- the elastomer comprises units of ethylene and units of an alkyl acrylate wherein the alkyl group contains 1-6 carbon atoms.
- the ethylene/alkyl acrylate copolymer contains 5-40 weight percent alkyl acrylate units, preferably 15-35 weight percent.
- the alkyl acrylates used in the ethylene/alkyl acrylate copolymers include methyl acrylate, ethyl acrylate, propyl acrylate, butyl acrylate, pentyl acrylate and hexyl acrylate. Preferably, methyl acrylate is used.
- the uncrosslinked elastomer contains as a cure site the monoalkyl esters of 1,4-butenedioic acid that reacts with the amine curing agent.
- the cure site monomers in the ethylene/alkyl acrylate elastomers are monoalkyl esters of 1,4-butenedioic acid in which the alkyl group generally contains 1-6 carbon atoms.
- butenedioic acids exist in the cis and trans form, i.e., maleic and fumaric acids
- the monoalkyl esters of either the cis or trans form are satisfactory.
- Representative monoalkyl esters of 1,4-butenedioic acid that are especially preferred are monoethyl hydrogen maleate, monoethyl hydrogen fumarate, monomethyl hydrogen maleate, monomethyl hydrogen fumarate, and monopropyl hydrogen maleate, and monoethyl hydrogen maleate is most especially preferred.
- the dynamically crosslinked ethylene/alkyl acrylate elastomers used in the compositions of the present invention can be prepared by direct copolymerization, for example, copolymerizing ethylene, an alkyl acrylate, and as a cure site the monoalkyl ester of 1,4-butenedioic acid, in the presence of a free-radical polymerization initiator at elevated temperatures, preferably 100°-270° C., and most preferably 130°-230° C., and at elevated pressures, preferably at least 70 MPa, and most preferably 140-350 MPa.
- the most preferred uncured ethylene/alkyl acrylates/monoalkyl ester of 1,4-butenedioic acid copolymers that are used to make the dynamically crosslinked elastomeric component of the thermoplastic blends of the present invention are copolymers of ethylene/methyl acrylate/monoethyl hydrogen maleate.
- Representative elastomers that can be dynamically crosslinked for use in this invention are described, for example, in U.S. Pat. No. 3,904,588.
- An important feature of the present invention is the necessity of dynamically crosslinking the high ethylene containing elastomeric ethylene, alkyl acrylate/monoalkyl ester of 1,4-butenedioic acid copolymer, usually, and most preferably, in the presence of the polyolefin resin. Dynamic crosslinking is carried out using one or more of the well known crosslinking agents for the ethylene/alkyl acrylate/monoalkyl esters of 1,4-butenedioic acid copolymers.
- Typical crosslinking agents that react with the cure sites of the ethylene, alkyl acrylate copolymers described herein include diamines or polyamines or precursors thereof such as methylenedianiline; 1,6-hexanediamine or its carbamate; meta-xylene-alpha,alpha'-diamine; 2-methyl-1,5-diamino-pentane; triethylenetetramine; diethylenetriamine; bis(para-aminocyclohexyl)methane; and ethylene diamine.
- the amount of crosslinking agent employed will vary over a wide range.
- crosslinking agent used usually results in a gel content of the dynamically crosslinked ethylene, alkyl acrylate copolymer of at least about 50 percent by weight.
- amounts of crosslinking agents range from about 0.1-5 parts by weight, usually 0.1-2 parts by weight, of the ethylene, alkyl acrylate elastomer containing cure sites.
- the amount of crosslinking agent used can be more than 5 parts by weight, there is no advantage in using larger amounts.
- optionally conventional promotors such as di-ortho-tolylguanidine, diphenylguanidine or the like can be used.
- the amount of insoluble, and hence crosslinked polymer is determined by leaching the sample of the crosslinked polymer at a temperature at which the polymer before crosslinking will dissolve in toluene, in the same toluene solvent for 48 hours, isolating the insoluble portion and weighing the dried polymer, making suitable corrections based upon knowledge of the composition. For example, the weight of additives soluble in toluene such as processing oils are subtracted from the initial weight. The weight of insoluble additives such as pigments, fillers etc., are subtracted from the initial and final weight. The portion of the crystalline polyolefin resin which is insoluble in toluene is subtracted from the initial and final weight.
- the insoluble polymer recovered after the required correction is reported as percent by weight gel content.
- the dynamically crosslinked elastomers of ethylene/alkyl acrylate usually have gel contents of at least about 50 percent by weight, preferably at least about 65 percent by weight.
- Conditions under which crosslinking is carried out, i.e., type and quantity of crosslinking agent, and crosslinking time and temperature, to arrive at a polymer having a gel content mentioned above can be determined empirically and is well known in the art of making crosslinked ethylene/alkyl acrylate elastomers.
- the multi-phase melt processible thermoplastic composition is prepared by mixing the crystalline polyolefin resin, the uncrosslinked ethylene/alkyl acrylate/monoalkyl ester of 1,4-butenedioic acid elastomer containing at least about 60 weight percent ethylene, preferably at least about 65 weight percent ethylene, and crosslinking agent, by any one of a number of well known procedures for mixing elastomers, for example, in a Banbury mixer, or in an extruder.
- the mixing is performed at a temperature high enough to soften the polymers for adequate mixing, but not so high as to degrade the polymers. Generally, mixing is performed at temperatures of from about 100°-280° C., usually about 125°-230° C.
- Crosslinking is conducted during mixing and shearing so as to dynamically crosslink the ethylene/alkyl acrylate copolymer containing cure sites.
- Mixing and shearing are carried out for a time sufficient to allow for dynamically crosslinking the ethylene/alkyl acrylate elastomer and for comminuting the crosslinked elastomer resulting in the elastomer being dispersed throughout the crystalline polyolefin resin.
- Adequacy of mixing can be determined by observing the processibility of the compositions by means of a piston rheometer.
- fillers and compounding ingredients are not essential components of the thermoplastic composition of this invention, preferably, especially from a cost standpoint, various amounts of conventional fillers and/or compounding ingredients normally used with elastomers are admixed with the compositions of this invention.
- suitable fillers and/or compounding ingredients normally used with elastomers are admixed with the compositions of this invention.
- examples of such ingredients include extending oils, e.g., aromatic oils, paraffinic oils or naphthenic oils; inorganic fillers, such as various carbon blacks, clays, silica, alumina, calcium carbonate; pigments, such as titanium dioxide; antioxidants; antidegradants; processing aids such as lubricants and waxes; and plasticizers such as dialkylphthalates, trialkylmellitates and dialkyladipates.
- thermoplastic composition it is preferable to add processing oils and/or plasticizers and inorganic fillers to the thermoplastic composition to improve its processing characteristics and the particular amounts used depend, at least in part, upon the quantities of other ingredients in the composition and the desired properties of the composition. Generally, amounts from about 5-50 parts by weight based on total polymers of fillers can be used and 10-100 parts by weight based on total weight of polymers of compounding ingredients such as processing oils and plasticizers can be used.
- the melt processible thermoplastic compositions of the subject invention can be processed using conventional plastic processing equipment.
- Articles molded from the thermoplastic compositions of the present invention exhibit properties generally only associated with vulcanized rubber.
- compositions of the present invention usually have tensile strength values of about 10-25 MPa and elongation at break values of about 100 to 350%.
- Various uses for the thermoplastic elastomer compositions include wire coverings, seals and gaskets, automotive parts, sheet liners and packaging films.
- melt processible thermoplastic compositions within the scope of this invention can be fabricated into tubing for laboratory, medical and industrial uses.
- Such tubing can also be used as the inner tube of reinforced hoses, wherein the extruded tube is overlaid with wire or textile cords, applied as a spiral, knit or braid.
- a polymeric covering can be applied (extruded, spiral wound or calendered sheet) over the reinforced tubing to provide protection from the working environment and mechanical abuse.
- Compositions within the scope of this invention can be used as the protective covering of reinforced tubes of similar or different composition.
- the polymers to be mixed were charged to a Brabender Plastograph mixer equipped with cam-style blades and modified to allow a flow of nitrogen gas to blanket the mixing chamber.
- the mixing chamber was preheated to the mixing temperatures given in the examples.
- the initial polymer composition for each example described below was mixed in the Brabender mixer until the temperature of the mixing chamber recovered to the preheat temperature. Mixing times given in the working examples were measured from that time forward. During preparation of the thermoplastic compositions, the temperature of the mixtures usually rose above the preset temperature of the mixing chamber. Specific details of the mixing procedures are described in the examples.
- Test specimens were cut from slabs molded at the temperatures specified in the examples to determine physical properties.
- the test methods used were:
- Compression sets were measured using 13 mm diameter discs died out of about 1.9 mm thick slabs and piled up to a thickness of about 13 mm. Specimens used for the oil swell tests were cut from 1.9 mm thick slabs. All tests were run in duplicate or triplicate.
- the polypropylene employed in the working examples hereinbelow is an isotactic homopolymer having a melt flow rate (ASTM D1238) at 230° C. of 0.8 dg/min and a density of 0.9 g/cm 3 .
- the polyethylene employed in the working examples hereinbelow is a high density polyethylene having a melt flow rate at 190° C. of 2.8 dg/min and a density of 0.96 g/cm 3 .
- the ethylene/alkyl acrylate elastomer employed contains ethylene, methyl acrylate, and the monoethyl hydrogen maleate.
- the ratio of ethylene to methyl acrylate was varied, as shown below in the tables.
- thermoplastic compositions described below in Table I were prepared from polypropylene homopolymer resin and the uncrosslinked elastomer of ethylene/methyl acrylate/cure site monomer in which the ratio of ethylene to methyl acrylate was varied as indicated below.
- the compositions were prepared by mixing 55 parts by weight polypropylene in the Brabender mixer for two minutes. When the temperature reached 180° C., 45 parts by weight elastomeric ethylene/methyl acrylate/cure site copolymer were added and mixing was continued for three minutes.
- thermoplastic composition was removed from the Brabender mixer, and sheeted off a roll mill at 170° C.
- the relative proportions of the polymer components, the composition of the ethylene/methyl acrylate cure site elastomer, the tensile strength and percent elongation of the thermoplastic compositions after compression molding at 220° C. are given below in Table I.
- Examples 1 to 3 are illustrative of the present invention illustrating the compatibility of the blends as shown by their high tensile strength and elongation at break.
- Comparative Example A illustrates that the blend with 41 weight percent ethylene units in the ethylene/methyl acrylate/cure site elastomer is not compatible and shows poor tensile strength and poor elongation at break values.
- thermoplastic compositions were prepared as described in Table II using polypropylene homopolymer resin, ethylene/methyl acrylate elastomer, calcined clay, paraffinic oil, and a plasticizer in the amounts indicated.
- the thermoplastic compositions were prepared by mixing the polypropylene in the Brabender mixer for two minutes. After the temperature reached 180° C., ethylene/methyl acrylate/cure site elastomer was added and mixing was continued for three minutes. The clay, paraffinic oil, and plasticizer were added slowly and the composition was mixed for an additional two minutes. The crosslinking agent triethylenetetramine was added and mixing and shearing of the composition was continued for 10 minutes to dynamically crosslink (i.e., cure) the elastomer. The resulting thermoplastic compositions were removed from the Brabender mixer and sheeted off a roll mill at 170° C.
- thermoplastic compositions described below in Table III were prepared as described above in Examples 1-3, and compression molded at 220° C. as described in Examples 1-3, except that the polypropylene homopolymer was replaced with high density polyethylene.
- the thermoplastic compositions were compression molded at 220° C. as described in Examples 1-3.
- Example 7 illustrates the compatibility of the blend as shown by its high tensile strength value and elongation at break value.
- Comparative Example E illustrates that the thermoplastic composition with only 41 weight percent ethylene units in the ethylene/methyl acrylate/cure site elastomer is less compatible with the polyethylene and has a poor tensile strength value and a poor E B value.
- thermoplastic compositions described below in Table IV were prepared as described above in Examples 1-3 but with the ratio of polyolefin resin to elastomer being varied.
- the properties of the thermoplastic composition after compression molding at 220° C. are given below in Table IV.
- Examples 8-11 demonstrate that the invention can be carried out at both high and low polyolefin concentrations, and the resulting blends are compatible as shown by their high tensile strength values and elongation at break values.
Abstract
Description
______________________________________ tensile strength at break ASTM D412 at 8.5 mm/s elongation at break ASTM D412 at 8.5 mm/s compression set ASTM D395 after 22 hr/100° C., method B volume swell in ASTM #3 oil ASTM D471 ______________________________________
TABLE I ______________________________________ Comp. Ex. 1 2 3 A ______________________________________ Polypropylene 55 55 55 55 64% E/32% MA/ 45 -- -- -- 4% MAME 69% E/27% MA/ -- 45 -- -- 4% MAME 79% E/17% MA/ -- -- 45 -- 4% MAME 41% E/55% MA/ -- -- -- 45 4% MAME Triethylene 0.9 0.9 0.9 0.9 tetramine Properties Tensile Strength, 25.0 25.2 23.6 14.5 MPa Elongation at 380 430 340 130 break, % ______________________________________ E/MA/MAME ethylene, methyl acrylate, monoethyl hydrogen maleate.
TABLE II ______________________________________ Comparative Examples 4 5 6 C D ______________________________________ Polypropylene 55 55 55 55 55 64% E/32% MA/ 45 -- -- -- -- 4% MAME 69% E/27% MA/ -- 45 -- -- -- 4% MAME 79% E/17% MA/ -- -- 45 -- -- 4% MAME 41% E/55% MA/ -- -- -- 45 -- 4% MAME 54% E/42% MA/ -- -- -- -- 45 4% MAME Calcined Clay 20 20 20 20 20 Paraffinic 20 20 20 20 20 Extender Oil Di(tridecyl)- 20 20 20 20 20 adipate plasticizer Triethylene- 0.9 0.9 0.9 0.9 0.9 tetramine Properties Tensile 11.4 11.7 12.3 5.7 7.3 Strength, MPa Elongation at 210 260 240 40 70 break, % Comp. set at 64 63 55 64 63 100° C., % Oil swell, 70 hrs. 38 45 47 -- 23 at 100° C., % ______________________________________ E/MA/MAME -- ethylene/methyl acrylate/monoethyl hydrogen maleate.
TABLE III ______________________________________ Comparative Example 7 E ______________________________________ Polyethylene 55 55 64% E/32% MA/4% MAME 45 41% E/55% MA/4% MAME 45 Triethylenetetramine 0.9 0.9 Properties Tensile strength, MPa 19.5 13.4 Elongation at break, % 370 155 ______________________________________ E/MA/MAME -- ethylene/methyl acrylate/monoethyl hydrogen maleate.
TABLE IV ______________________________________ 8 9 10 11 ______________________________________ polypropylene, 25 -- 65 -- parts by weight polyethylene, -- 25 -- 65 parts by weight 64% ethylene/32% methyl 75 75 35 35 acrylate/4% MAME* elastomer, parts by weight triethylenetetramine, 0.5 0.5 1.3 1.3 parts by weight Tensile Properties Tensile strength, MPa 22.9 15.2 21.0 18.3 Elongation at break, % 550 320 305 285 ______________________________________ *MAME -- monoethyl hydrogen maleate.
Claims (26)
Priority Applications (8)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US07/017,332 US4710544A (en) | 1985-11-07 | 1987-02-20 | Thermoplastic composition of polyolefin and high ethylene content ethylene/alkyl acrylate elastomer |
NO874252A NO874252L (en) | 1987-02-20 | 1987-10-12 | THERMOPLASTIC MATERIAL BASED ON POLYOLEFINE AND AN ETHYLENE / ALKYLACRYLATE ELASTOMER WITH HIGH ETHYLENE CONTENT. |
DK535787A DK535787A (en) | 1987-02-20 | 1987-10-13 | THERMOPLASTIC COMPOSITION OF POLYOLEFINE AND ETHYLENE / ALKYLACRYLATE ELASTOMES WITH HIGH ETHYLENE CONTENTS PREPARED THEREOF |
AU79756/87A AU7975687A (en) | 1987-02-20 | 1987-10-14 | Polyolefin and ethylene/alkyl acrylate polymer composition |
EP87114997A EP0279026A3 (en) | 1987-02-20 | 1987-10-14 | Thermoplastic composition of polyolefin and high ethylene content ethylene/alkyl acrylate elastomer |
BR8705614A BR8705614A (en) | 1987-02-20 | 1987-10-20 | THERMOPLASTIC COMPOSITION THROUGH FUSION AND PROCESS FOR ITS MANUFACTURING |
KR1019870011749A KR910000942B1 (en) | 1987-02-20 | 1987-10-22 | Thermoplastic composition of polyolefin and high ethylene content ethylene/alkyl acrylate elastomer |
JP62266655A JPS63205337A (en) | 1987-02-20 | 1987-10-23 | Melt processable thermoplastic composition |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US06/796,589 US4782110A (en) | 1985-11-07 | 1985-11-07 | Thermoplastic compositions of crystalline polyolefin, and ethylene/alkyl acrylate copolymer elastomer |
US07/017,332 US4710544A (en) | 1985-11-07 | 1987-02-20 | Thermoplastic composition of polyolefin and high ethylene content ethylene/alkyl acrylate elastomer |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
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US06/796,589 Continuation-In-Part US4782110A (en) | 1985-11-07 | 1985-11-07 | Thermoplastic compositions of crystalline polyolefin, and ethylene/alkyl acrylate copolymer elastomer |
Publications (1)
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US4710544A true US4710544A (en) | 1987-12-01 |
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Application Number | Title | Priority Date | Filing Date |
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US07/017,332 Expired - Lifetime US4710544A (en) | 1985-11-07 | 1987-02-20 | Thermoplastic composition of polyolefin and high ethylene content ethylene/alkyl acrylate elastomer |
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US (1) | US4710544A (en) |
EP (1) | EP0279026A3 (en) |
JP (1) | JPS63205337A (en) |
KR (1) | KR910000942B1 (en) |
AU (1) | AU7975687A (en) |
BR (1) | BR8705614A (en) |
DK (1) | DK535787A (en) |
NO (1) | NO874252L (en) |
Cited By (23)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4775722A (en) * | 1986-09-17 | 1988-10-04 | Nippon Oil Company, Limited | Thermoplastic elastomer compositions |
US4782110A (en) * | 1985-11-07 | 1988-11-01 | E. I. Du Pont De Nemours And Company | Thermoplastic compositions of crystalline polyolefin, and ethylene/alkyl acrylate copolymer elastomer |
EP0311332A2 (en) * | 1987-10-05 | 1989-04-12 | Nippon Zeon Co., Ltd. | Rubber composition |
WO1989004346A1 (en) * | 1987-11-13 | 1989-05-18 | E.I. Du Pont De Nemours And Company | Flexible thermoplastic composition |
US4871810A (en) * | 1987-11-13 | 1989-10-03 | E. I. Du Pont De Nemours And Company | Composition comprising melt blended product of thermoplastic resin and two ethylene copolymers containing coreactive groups |
US4933389A (en) * | 1988-02-03 | 1990-06-12 | Sumitomo Chemical Company, Limited | Thermoplastic elastomer composition |
US5013877A (en) * | 1988-02-08 | 1991-05-07 | Raychem Corporation | Devices for electrical connection |
US5077129A (en) * | 1990-03-01 | 1991-12-31 | Wolff Walsrode Ag | Stretched polypropylene films having good surface slip |
US5360874A (en) * | 1992-06-03 | 1994-11-01 | J. H. Benecke Ag | Sintered film |
WO1995032241A1 (en) * | 1994-05-19 | 1995-11-30 | E.I. Du Pont De Nemours And Company | Curable ethylene copolymer blend composition |
WO1998054254A1 (en) * | 1997-05-27 | 1998-12-03 | Optatech Corporation | Process for preparing polyacrylate/polyolefin blends |
US5889118A (en) * | 1996-06-03 | 1999-03-30 | Minnesota Mining And Manufacturing Company | Thermomorphic "smart" pressure sensitive adhesives |
US5986000A (en) * | 1995-05-22 | 1999-11-16 | Playtex Products, Inc. | Soft, flexible composition and method for making same |
EP1408079A1 (en) * | 2002-10-09 | 2004-04-14 | The Goodyear Tire & Rubber Company | Hose construction containing polymer composition |
US20060094807A1 (en) * | 2004-09-09 | 2006-05-04 | Prejean George W | Injectable moldable thermoplastic compositions |
US20060275610A1 (en) * | 2001-06-04 | 2006-12-07 | Saint-Gobain Performance Plastics Corporation | Multi-layer release films |
US20070049682A1 (en) * | 2005-09-01 | 2007-03-01 | Walsh David J | Soft polymer compositions having improved high temperature properties |
US20070190335A1 (en) * | 2006-02-13 | 2007-08-16 | Saint-Gobain Performance Plastics Corporation | Multi-layer release films |
US20070202311A1 (en) * | 2006-02-28 | 2007-08-30 | Saint-Gobain Performance Plastics Corporation | Multi-layer release films |
US20070206364A1 (en) * | 2006-03-02 | 2007-09-06 | Saint-Gobain Performance Plastics Corporation | Methods of forming a flexible circuit board |
US10351749B2 (en) * | 2015-06-18 | 2019-07-16 | Dow Global Technologies Llc | Thermally conductive elastomeric composites |
EP3578580A4 (en) * | 2017-01-31 | 2020-07-22 | Zeon Corporation | Acrylic rubber, acrylic rubber composition, and acrylic rubber crosslinked product |
WO2023240938A1 (en) * | 2022-06-17 | 2023-12-21 | 中国石油天然气股份有限公司 | Reversibly crosslinked polyethylene cable material and preparation method therefor |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5936038A (en) * | 1996-08-09 | 1999-08-10 | The University Of Akron | Vulcanizable elastomeric composition and thermoplastic vulcanizate employing the same |
CZ2013204A3 (en) * | 2013-03-22 | 2014-05-07 | Vysoká Škola Báňská-Technická Univerzita Ostrava | Rotary vane feeder for bulk material fluidization and fluidization process of bulk material |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2953541A (en) * | 1958-06-16 | 1960-09-20 | Union Carbide Corp | Composition of polyethylene and a copolymer of ethylene and ethyl acrylate |
US3904588A (en) * | 1973-08-09 | 1975-09-09 | Du Pont | Random ethylene/alkyl acrylate 1,4-butene-dioic acid terpolymers |
US4234656A (en) * | 1978-12-20 | 1980-11-18 | Union Carbide Corporation | Reprocessable thermoplastic graft copolymer of propylene polymer and ethylene copolymer |
US4275180A (en) * | 1977-04-12 | 1981-06-23 | Raychem Limited | Polymer compositions |
US4555546A (en) * | 1983-12-29 | 1985-11-26 | Monsanto Company | Compatibilized blends of acrylic ester |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NZ216138A (en) * | 1985-05-21 | 1989-01-27 | Bp Chem Int Ltd | Thermoplastic, low smoke and flame retardant acrylate rubber-polyolefin resin composition |
-
1987
- 1987-02-20 US US07/017,332 patent/US4710544A/en not_active Expired - Lifetime
- 1987-10-12 NO NO874252A patent/NO874252L/en unknown
- 1987-10-13 DK DK535787A patent/DK535787A/en not_active Application Discontinuation
- 1987-10-14 AU AU79756/87A patent/AU7975687A/en not_active Abandoned
- 1987-10-14 EP EP87114997A patent/EP0279026A3/en not_active Withdrawn
- 1987-10-20 BR BR8705614A patent/BR8705614A/en unknown
- 1987-10-22 KR KR1019870011749A patent/KR910000942B1/en active IP Right Grant
- 1987-10-23 JP JP62266655A patent/JPS63205337A/en active Pending
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2953541A (en) * | 1958-06-16 | 1960-09-20 | Union Carbide Corp | Composition of polyethylene and a copolymer of ethylene and ethyl acrylate |
US3904588A (en) * | 1973-08-09 | 1975-09-09 | Du Pont | Random ethylene/alkyl acrylate 1,4-butene-dioic acid terpolymers |
US4275180A (en) * | 1977-04-12 | 1981-06-23 | Raychem Limited | Polymer compositions |
US4234656A (en) * | 1978-12-20 | 1980-11-18 | Union Carbide Corporation | Reprocessable thermoplastic graft copolymer of propylene polymer and ethylene copolymer |
US4555546A (en) * | 1983-12-29 | 1985-11-26 | Monsanto Company | Compatibilized blends of acrylic ester |
Cited By (37)
Publication number | Priority date | Publication date | Assignee | Title |
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US4782110A (en) * | 1985-11-07 | 1988-11-01 | E. I. Du Pont De Nemours And Company | Thermoplastic compositions of crystalline polyolefin, and ethylene/alkyl acrylate copolymer elastomer |
US4775722A (en) * | 1986-09-17 | 1988-10-04 | Nippon Oil Company, Limited | Thermoplastic elastomer compositions |
EP0311332A3 (en) * | 1987-10-05 | 1990-05-23 | Nippon Zeon Co., Ltd. | Rubber composition |
EP0311332A2 (en) * | 1987-10-05 | 1989-04-12 | Nippon Zeon Co., Ltd. | Rubber composition |
US4871810A (en) * | 1987-11-13 | 1989-10-03 | E. I. Du Pont De Nemours And Company | Composition comprising melt blended product of thermoplastic resin and two ethylene copolymers containing coreactive groups |
WO1989004346A1 (en) * | 1987-11-13 | 1989-05-18 | E.I. Du Pont De Nemours And Company | Flexible thermoplastic composition |
US4933389A (en) * | 1988-02-03 | 1990-06-12 | Sumitomo Chemical Company, Limited | Thermoplastic elastomer composition |
US5013877A (en) * | 1988-02-08 | 1991-05-07 | Raychem Corporation | Devices for electrical connection |
US5077129A (en) * | 1990-03-01 | 1991-12-31 | Wolff Walsrode Ag | Stretched polypropylene films having good surface slip |
US5360874A (en) * | 1992-06-03 | 1994-11-01 | J. H. Benecke Ag | Sintered film |
WO1995032241A1 (en) * | 1994-05-19 | 1995-11-30 | E.I. Du Pont De Nemours And Company | Curable ethylene copolymer blend composition |
US5498669A (en) * | 1994-05-19 | 1996-03-12 | E. I. Du Pont De Nemours And Company | Curable ethylene copolymer blend composition |
US6254565B1 (en) | 1995-05-22 | 2001-07-03 | Playtex Products, Inc. | Soft, flexible composition and method for making same |
US5986000A (en) * | 1995-05-22 | 1999-11-16 | Playtex Products, Inc. | Soft, flexible composition and method for making same |
US5889118A (en) * | 1996-06-03 | 1999-03-30 | Minnesota Mining And Manufacturing Company | Thermomorphic "smart" pressure sensitive adhesives |
US6060159A (en) * | 1996-06-03 | 2000-05-09 | Delgado; Joaquin | Thermomorphic "smart" pressure sensitive adhesives |
CN1125133C (en) * | 1997-05-27 | 2003-10-22 | 南京金陵奥普特高分子材料有限公司 | Process for preparing polyacrylate/polyolefin blends |
US6262177B1 (en) | 1997-05-27 | 2001-07-17 | Optatech Corporation | Process for preparing polyacrylate/polyolefin blends |
WO1998054254A1 (en) * | 1997-05-27 | 1998-12-03 | Optatech Corporation | Process for preparing polyacrylate/polyolefin blends |
US7776446B2 (en) | 2001-06-04 | 2010-08-17 | Saint-Gobain Performance Plastics Corporation | Multi-layer release films |
US20060275610A1 (en) * | 2001-06-04 | 2006-12-07 | Saint-Gobain Performance Plastics Corporation | Multi-layer release films |
US7371446B2 (en) | 2002-10-09 | 2008-05-13 | Veyance Technologies, Inc. | Hose construction containing polymer composition |
EP1408079A1 (en) * | 2002-10-09 | 2004-04-14 | The Goodyear Tire & Rubber Company | Hose construction containing polymer composition |
US20040071911A1 (en) * | 2002-10-09 | 2004-04-15 | Kerstetter Randal Howard | Hose construction containing polymer composition |
US20060094807A1 (en) * | 2004-09-09 | 2006-05-04 | Prejean George W | Injectable moldable thermoplastic compositions |
WO2007027862A2 (en) * | 2005-09-01 | 2007-03-08 | E. I. Du Pont De Nemours And Company | Soft polymer compositions having improved high temperature properties |
WO2007027862A3 (en) * | 2005-09-01 | 2007-04-26 | Du Pont | Soft polymer compositions having improved high temperature properties |
US7655731B2 (en) * | 2005-09-01 | 2010-02-02 | E.I. Du Pont De Nemours And Company | Soft polymer compositions having improved high temperature properties |
US20070049682A1 (en) * | 2005-09-01 | 2007-03-01 | Walsh David J | Soft polymer compositions having improved high temperature properties |
CN101253239B (en) * | 2005-09-01 | 2011-04-13 | 纳幕尔杜邦公司 | Soft polymer compositions having improved high temperature properties |
US20070190335A1 (en) * | 2006-02-13 | 2007-08-16 | Saint-Gobain Performance Plastics Corporation | Multi-layer release films |
US7776428B2 (en) | 2006-02-13 | 2010-08-17 | Saint-Gobain Performance Plastics Corporation | Multi-layer release films |
US20070202311A1 (en) * | 2006-02-28 | 2007-08-30 | Saint-Gobain Performance Plastics Corporation | Multi-layer release films |
US20070206364A1 (en) * | 2006-03-02 | 2007-09-06 | Saint-Gobain Performance Plastics Corporation | Methods of forming a flexible circuit board |
US10351749B2 (en) * | 2015-06-18 | 2019-07-16 | Dow Global Technologies Llc | Thermally conductive elastomeric composites |
EP3578580A4 (en) * | 2017-01-31 | 2020-07-22 | Zeon Corporation | Acrylic rubber, acrylic rubber composition, and acrylic rubber crosslinked product |
WO2023240938A1 (en) * | 2022-06-17 | 2023-12-21 | 中国石油天然气股份有限公司 | Reversibly crosslinked polyethylene cable material and preparation method therefor |
Also Published As
Publication number | Publication date |
---|---|
NO874252D0 (en) | 1987-10-12 |
KR880010047A (en) | 1988-10-06 |
AU7975687A (en) | 1988-08-25 |
DK535787D0 (en) | 1987-10-13 |
EP0279026A3 (en) | 1990-03-21 |
NO874252L (en) | 1988-08-22 |
EP0279026A2 (en) | 1988-08-24 |
KR910000942B1 (en) | 1991-02-19 |
DK535787A (en) | 1988-08-21 |
JPS63205337A (en) | 1988-08-24 |
BR8705614A (en) | 1988-09-13 |
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